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Common Coding brings Clarity to Medical Device Regulations

The Global Medical Device Nomenclature (GMDN) has joined forces with the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) to strengthen the functionality of the MHRAs Public Access Registration Database (PARD), a significant development for medical device regulation that will improve patient safety, streamline the classification, promote transparency and enhance accessibility to vital medical device information. Click to read more...
United Kingdom Laura Squire Deniz Bruce Regulatory Agency Global Medical Device Nomenclature Access Registration Database

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